JP2000169385A - Internal liquid pharmaceutical preparation - Google Patents
Internal liquid pharmaceutical preparationInfo
- Publication number
- JP2000169385A JP2000169385A JP10351800A JP35180098A JP2000169385A JP 2000169385 A JP2000169385 A JP 2000169385A JP 10351800 A JP10351800 A JP 10351800A JP 35180098 A JP35180098 A JP 35180098A JP 2000169385 A JP2000169385 A JP 2000169385A
- Authority
- JP
- Japan
- Prior art keywords
- iron
- component
- mmol
- citrate
- xylitol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 24
- 239000000825 pharmaceutical preparation Substances 0.000 title abstract 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 86
- 229910052742 iron Inorganic materials 0.000 claims abstract description 43
- 238000002360 preparation method Methods 0.000 claims abstract description 19
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims abstract description 16
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000000811 xylitol Substances 0.000 claims abstract description 16
- 235000010447 xylitol Nutrition 0.000 claims abstract description 16
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims abstract description 16
- 229960002675 xylitol Drugs 0.000 claims abstract description 16
- NPFOYSMITVOQOS-UHFFFAOYSA-K iron(III) citrate Chemical compound [Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NPFOYSMITVOQOS-UHFFFAOYSA-K 0.000 claims abstract description 4
- KXFFQVUPQCREHA-UHFFFAOYSA-K sodium;2-hydroxypropane-1,2,3-tricarboxylate;iron(2+) Chemical compound [Na+].[Fe+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KXFFQVUPQCREHA-UHFFFAOYSA-K 0.000 claims abstract description 4
- 229940100688 oral solution Drugs 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- GLMQHZPGHAPYIO-UHFFFAOYSA-L azanium;2-hydroxypropane-1,2,3-tricarboxylate;iron(2+) Chemical compound [NH4+].[Fe+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O GLMQHZPGHAPYIO-UHFFFAOYSA-L 0.000 claims description 3
- 239000004222 ferrous gluconate Substances 0.000 claims description 3
- 235000013924 ferrous gluconate Nutrition 0.000 claims description 3
- 229960001645 ferrous gluconate Drugs 0.000 claims description 3
- 239000004313 iron ammonium citrate Substances 0.000 claims description 3
- 235000000011 iron ammonium citrate Nutrition 0.000 claims description 3
- VRIVJOXICYMTAG-IYEMJOQQSA-L iron(ii) gluconate Chemical compound [Fe+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O VRIVJOXICYMTAG-IYEMJOQQSA-L 0.000 claims description 3
- 239000003814 drug Substances 0.000 abstract description 20
- 229940079593 drug Drugs 0.000 abstract description 17
- 208000025371 Taste disease Diseases 0.000 abstract description 15
- 235000019656 metallic taste Nutrition 0.000 abstract description 15
- PLKYGPRDCKGEJH-UHFFFAOYSA-N azane;2-hydroxypropane-1,2,3-tricarboxylic acid;iron Chemical compound N.[Fe].OC(=O)CC(O)(C(O)=O)CC(O)=O PLKYGPRDCKGEJH-UHFFFAOYSA-N 0.000 abstract description 9
- 208000007502 anemia Diseases 0.000 abstract description 4
- 235000013361 beverage Nutrition 0.000 abstract description 2
- 235000020357 syrup Nutrition 0.000 abstract description 2
- 239000006188 syrup Substances 0.000 abstract description 2
- 230000002265 prevention Effects 0.000 abstract 1
- 239000000284 extract Substances 0.000 description 13
- 238000011156 evaluation Methods 0.000 description 8
- 239000008213 purified water Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229940088594 vitamin Drugs 0.000 description 6
- 229930003231 vitamin Natural products 0.000 description 6
- 235000013343 vitamin Nutrition 0.000 description 6
- 239000011782 vitamin Substances 0.000 description 6
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 5
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 239000001630 malic acid Substances 0.000 description 4
- 235000011090 malic acid Nutrition 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 206010016326 Feeling cold Diseases 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 230000000873 masking effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 235000013355 food flavoring agent Nutrition 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000003002 pH adjusting agent Substances 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 235000019640 taste Nutrition 0.000 description 2
- 150000003722 vitamin derivatives Chemical class 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- YNVZDODIHZTHOZ-UHFFFAOYSA-K 2-hydroxypropanoate;iron(3+) Chemical compound [Fe+3].CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O YNVZDODIHZTHOZ-UHFFFAOYSA-K 0.000 description 1
- AEDORKVKMIVLBW-BLDDREHASA-N 3-oxo-3-[[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-[[5-hydroxy-4-(hydroxymethyl)-6-methylpyridin-3-yl]methoxy]oxan-2-yl]methoxy]propanoic acid Chemical compound OCC1=C(O)C(C)=NC=C1CO[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](COC(=O)CC(O)=O)O1 AEDORKVKMIVLBW-BLDDREHASA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 102000008857 Ferritin Human genes 0.000 description 1
- 238000008416 Ferritin Methods 0.000 description 1
- 108050000784 Ferritin Proteins 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 1
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 102000036675 Myoglobin Human genes 0.000 description 1
- 108010062374 Myoglobin Proteins 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 101001094026 Synechocystis sp. (strain PCC 6803 / Kazusa) Phasin PhaP Proteins 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003270 Vitamin B Natural products 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 229930003316 Vitamin D Natural products 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229940024606 amino acid Drugs 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- DFGZNZXWHOAMEH-UHFFFAOYSA-N butyl benzoate;propyl benzoate Chemical compound CCCOC(=O)C1=CC=CC=C1.CCCCOC(=O)C1=CC=CC=C1 DFGZNZXWHOAMEH-UHFFFAOYSA-N 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 239000011706 ferric diphosphate Substances 0.000 description 1
- 235000007144 ferric diphosphate Nutrition 0.000 description 1
- CADNYOZXMIKYPR-UHFFFAOYSA-B ferric pyrophosphate Chemical compound [Fe+3].[Fe+3].[Fe+3].[Fe+3].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O CADNYOZXMIKYPR-UHFFFAOYSA-B 0.000 description 1
- 229940036404 ferric pyrophosphate Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- FVTCRASFADXXNN-SCRDCRAPSA-N flavin mononucleotide Chemical compound OP(=O)(O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O FVTCRASFADXXNN-SCRDCRAPSA-N 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000008369 fruit flavor Substances 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 230000010030 glucose lowering effect Effects 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229940064880 inositol 100 mg Drugs 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- ATEAWHILRRXHPW-UHFFFAOYSA-J iron(2+);phosphonato phosphate Chemical compound [Fe+2].[Fe+2].[O-]P([O-])(=O)OP([O-])([O-])=O ATEAWHILRRXHPW-UHFFFAOYSA-J 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 230000002475 laxative effect Effects 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- RXMQCXCANMAVIO-CEOVSRFSSA-L magnesium;(2s)-2-amino-4-hydroxy-4-oxobutanoate Chemical compound [H+].[H+].[Mg+2].[O-]C(=O)[C@@H](N)CC([O-])=O.[O-]C(=O)[C@@H](N)CC([O-])=O RXMQCXCANMAVIO-CEOVSRFSSA-L 0.000 description 1
- 206010025482 malaise Diseases 0.000 description 1
- 235000019663 masking metalicness Nutrition 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940089808 pyridoxine hydrochloride 10 mg Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229950001574 riboflavin phosphate Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- UIERGBJEBXXIGO-UHFFFAOYSA-N thiamine mononitrate Chemical compound [O-][N+]([O-])=O.CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N UIERGBJEBXXIGO-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 239000009538 yokuinin Substances 0.000 description 1
Abstract
Description
【0001】[0001]
【発明が属する技術分野】本発明は、鉄成分と地黄を配
合した液剤において鉄由来の金属味が軽減された内服液
剤に関するものであり、医薬、食品の分野に応用できる
ものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a liquid preparation containing an iron component and ground yellow in which the metallic taste derived from iron is reduced, and is applicable to the fields of medicine and food.
【0002】[0002]
【従来の技術】鉄は、主に血液中のヘモグロビン、筋肉
中のミオグロビン、肝臓のフェリチンなど、生体内に広
く分布し、不足すると貧血や倦怠感などの症状をひき起
こす。また、地黄は、血糖下降作用、抗血管内凝固作
用、血流改善効果などがあり、冷え性などの改善に効果
がある生薬である。貧血や冷え性などは女性に多くみら
れる症状であり、従って鉄と地黄を同時に配合する薬剤
は特に女性用の医薬として有用である。しかしながら、
鉄成分を内服液剤に配合した場合には、その独特の金属
味ゆえに服用しにくいという欠点があった。2. Description of the Related Art Iron is widely distributed in living organisms, such as hemoglobin in blood, myoglobin in muscle, and ferritin in liver. If iron is insufficient, it causes symptoms such as anemia and malaise. In addition, ground yellow has a blood glucose lowering action, an anti-intravascular coagulation action, a blood flow improving effect, and the like, and is a crude drug that is effective in improving coldness and the like. Anemia, chilliness and the like are symptoms that are common in women. Therefore, a drug containing iron and ground yellow at the same time is particularly useful as a medicine for women. However,
When an iron component is incorporated into an oral solution, there is a drawback that it is difficult to take due to its unique metallic taste.
【0003】このような鉄由来の金属味を改善する方法
としては、フルーツジュースを配合する方法(特開昭6
4−86858号公報)、アルコール成分を配合する方
法(特開平4−27369号公報)、香料を配合する方
法などが知られているが、必ずしも十分なものではな
い。[0003] As a method of improving such metallic taste derived from iron, a method of blending fruit juice (Japanese Patent Application Laid-Open No.
JP-A-4-86858), a method of blending an alcohol component (JP-A-4-27369), and a method of blending a fragrance are known, but are not necessarily sufficient.
【0004】一方、地黄にはそれ自身に金属味をマスキ
ングする効果があり、鉄成分を含む内服液剤に地黄を配
合することは有用である。しかしながら、低濃度の鉄成
分を含む内服液剤の場合には有用であっても、高濃度の
場合には必ずしも充分なマスキング効果が得られないと
いう問題点がある。On the other hand, ground yellow has an effect of masking metallic taste to itself, and it is useful to mix ground yellow with an oral solution containing an iron component. However, there is a problem that even if the liquid preparation containing an iron component at a low concentration is useful, a sufficient masking effect cannot always be obtained at a high concentration.
【0005】[0005]
【発明が解決しようとする課題】本発明の目的は、鉄成
分と地黄を配合し、鉄由来の金属味をマスキングした、
貧血や冷え性などの治療又は予防に対して極めて有効な
内服液剤を提供することである。SUMMARY OF THE INVENTION An object of the present invention is to mix an iron component and ground yellow to mask the metallic taste derived from iron.
It is an object of the present invention to provide an oral solution which is extremely effective for treating or preventing anemia and chilliness.
【0006】[0006]
【課題を解決するための手段】本発明者らは、上記目的
を達するため鋭意研究を進めた結果、鉄成分と地黄を配
合した内服液剤において新たにキシリトールを配合する
ことにより課題を解決することを見いだし、本発明を完
成した。すなわち、本発明は鉄成分、地黄及びキシリト
ールを含有することを特徴とする内服液剤である。Means for Solving the Problems The present inventors have made intensive studies to achieve the above object, and as a result, have solved the problem by adding a new xylitol to an oral solution containing an iron component and ground yellow. And completed the present invention. That is, the present invention is an oral liquid preparation characterized by containing an iron component, ground yellow and xylitol.
【0007】[0007]
【発明の実施の形態】本発明において、鉄成分はクエン
酸鉄、クエン酸鉄アンモニウム、クエン酸鉄ナトリウ
ム、グルコン酸第一鉄、乳酸鉄、ピロリン酸第一鉄、ピ
ロリン酸第二鉄、硫酸第一鉄、塩化第二鉄など、内服液
剤に配合可能な鉄含有化合物であれば特に限定されない
が、クエン酸鉄、クエン酸鉄アンモニウム及びクエン酸
鉄ナトリウム、グルコン酸第一鉄でより本発明の効果が
発揮され、更にクエン酸鉄アンモニウムでより本発明の
効果が発揮される。鉄成分は、鉄量として50mmol/L以
下の割合で配合した場合本発明の効果が発現するが、鉄
量が0.05mmol/L以下の薄い領域では、本発明に依ら
ずマスキングが可能であり、濃い領域では効果が低くな
る。好ましくは0.1〜30mmol/Lの範囲であ
る。BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, iron components are iron citrate, iron ammonium citrate, iron sodium citrate, ferrous gluconate, iron lactate, ferrous pyrophosphate, ferric pyrophosphate, and sulfuric acid. There is no particular limitation as long as it is an iron-containing compound, such as ferrous iron or ferric chloride, which can be blended in the oral liquid, but the present invention is more preferable with iron citrate, iron ammonium citrate and sodium iron citrate, and ferrous gluconate. And the effect of the present invention is further exhibited by ammonium iron citrate. Although the effect of the present invention is exhibited when the iron component is blended at a rate of 50 mmol / L or less as the iron content, masking is possible regardless of the present invention in a thin region where the iron content is 0.05 mmol / L or less. In a dark area, the effect is low. Preferably, it is in the range of 0.1 to 30 mmol / L.
【0008】本発明に用いる地黄は生地黄、鮮地黄、乾
地黄、熟地黄など、及びそられを原料とし通常の方法に
より製造された乾燥エキス、軟エキス、流エキス、抽出
液であり、一般に市販されているものも使用することが
できる。地黄の配合量は、それ自身に薬効及びマスキン
グ効果があることから、原生薬換算量として10〜40
00mg、好ましくは40〜2000mgを1回服用量とし
て配合することができる。10mg以下だとその効果が期
待できず、4000mgを越えて配合することは地黄自身
の味が強く風味が損なわれるからである。[0008] The ground yellow used in the present invention is dough yellow, fresh ground yellow, dry ground yellow, mature ground yellow, etc., and dry extracts, soft extracts, flow extracts, and extracts prepared from the raw materials by the usual methods. Commercially available ones can also be used. The amount of ground yellow is 10 to 40 as a crude drug equivalent, since it has a medicinal effect and a masking effect by itself.
00 mg, preferably 40-2000 mg, can be formulated as a single dose. If the amount is less than 10 mg, the effect cannot be expected, and if it exceeds 4000 mg, the ground yellow itself has a strong taste and the flavor is impaired.
【0009】キシリトールは、鉄量1mmolに対しキシリ
トール20mmol以上配合することにより鉄と地黄配合下
における鉄由来の金属味をマスキングできるが、好まし
くは30mmol以上である。また、キシリトールは緩下作
用があることから、1回服用量は20g以下が好まし
い。Xylitol can mask a metallic taste derived from iron in a mixture of iron and ground yellow by adding 20 mmol or more of xylitol to 1 mmol of iron, but is preferably 30 mmol or more. In addition, since xylitol has a laxative effect, a single dose is preferably 20 g or less.
【0010】また、本発明の内服液剤には他にビタミン
類、例えばビタミンB群、ビタミンC類などの水溶性ビ
タミン、ビタミンA類、ビタミンD類、ビタミンE類な
どの脂溶性ビタミンなどを含んでも良い。これらのビタ
ミン類は、一種又は二種以上使用できる。The oral liquid preparation of the present invention also contains vitamins, for example, water-soluble vitamins such as vitamin B group and vitamin C, and fat-soluble vitamins such as vitamin A, vitamin D and vitamin E. But it is good. One or more of these vitamins can be used.
【0011】本発明の内服液剤のpHは通常2〜7程
度、好ましくは2.5〜6程度である。内服液剤のpH
は繁用のpH調整剤を用いて調整できる。pH調整剤と
しては、例えばクエン酸、リンゴ酸、酒石酸、フマル
酸、乳酸、コハク酸、アスコルビン酸、酢酸などの有機
酸及びそれらの塩類、塩酸、リン酸などの無機酸及びそ
れらの塩類などが挙げられる。これらのpH調整剤は一
種又は二種以上使用できる。The pH of the liquid preparation of the present invention is usually about 2 to 7, preferably about 2.5 to 6. PH of oral solution
Can be adjusted using a conventional pH adjuster. Examples of the pH adjuster include organic acids and salts thereof such as citric acid, malic acid, tartaric acid, fumaric acid, lactic acid, succinic acid, ascorbic acid, and acetic acid; and inorganic acids and salts thereof such as hydrochloric acid and phosphoric acid. No. One or more of these pH adjusters can be used.
【0012】また、本発明の内服液剤には、その他の成
分としてミネラル、アミノ酸及びその塩類、生薬及び生
薬抽出物、甘味剤、保存剤、矯味剤、着香剤、着色剤な
ど、内服液剤一般に使用される成分を配合することがで
きる。The oral liquid preparation of the present invention generally contains, as other components, minerals, amino acids and salts thereof, crude drugs and crude drug extracts, sweeteners, preservatives, flavoring agents, flavoring agents, coloring agents and the like. The components used can be blended.
【0013】本発明かかわる内服液剤は、常法により調
製でき、その方法は特に制限はされないが、通常、各成
分を規定量以下の精製水にて混合し、規定量に容量調整
し、必要に応じて濾過、滅菌処理をすることにより得ら
れる。なお、脂溶性ビタミンを含むときは、通常用いら
れる界面活性剤又は可溶化剤により乳化又は可溶化して
もよく、また分散剤を用いて懸濁させても良い。The liquid preparation for internal use according to the present invention can be prepared by a conventional method, and the method is not particularly limited. Usually, each component is mixed with a specified amount or less of purified water, and the volume is adjusted to the specified amount. It is obtained by performing filtration and sterilization as appropriate. When a fat-soluble vitamin is contained, the fat-soluble vitamin may be emulsified or solubilized with a commonly used surfactant or solubilizer, or may be suspended with a dispersant.
【0014】本発明の内服液剤は、例えばドリンク剤、
シロップ剤などの医薬品や医薬部外品の内服液剤、健康
飲料などの各種飲料に適用できる。The oral liquid preparation of the present invention is, for example, a drink preparation,
The present invention can be applied to various kinds of beverages such as medicines such as syrups, oral liquids of quasi-drugs, and health drinks.
【0015】[0015]
【発明の効果】鉄成分と地黄を配合した内服液剤におい
て、更にキシリトールを配合することにより鉄由来の金
属味を有効に軽減し服用し易い内服液剤を提供できるこ
とを見出した。According to the present invention, it has been found that, by further mixing xylitol in an oral solution containing an iron component and ground yellow, an oral solution which can effectively reduce the metallic taste derived from iron and is easy to take can be provided.
【0016】[0016]
【実施例】次に、本発明を実施例及び試験例を挙げて詳
細に説明する。 実施例1 クエン酸鉄アンモニウム 40 mg 地黄エキス 200 mg(原生薬換算) キシリトール 2000 mg 精製水 (全量) 100 mL (鉄量として約1.2mmol/L) 上記成分を混合溶解し液剤を得た。Next, the present invention will be described in detail with reference to examples and test examples. Example 1 Ammonium iron citrate 40 mg Ground yellow extract 200 mg (equivalent to crude drug) Xylitol 2000 mg Purified water (total) 100 mL (about 1.2 mmol / L as iron) The above components were mixed and dissolved to obtain a liquid preparation.
【0017】 実施例2 クエン酸鉄アンモニウム 40 mg 地黄エキス 200 mg(原生薬換算) キシリトール 2000 mg リンゴ酸 適量 (pH4) 精製水 (全量) 100 mL (鉄量として約1.2mmol/L) 上記成分を混合溶解し液剤を得た。Example 2 Ammonium iron citrate 40 mg Ground yellow extract 200 mg (converted to crude drug) Xylitol 2000 mg Malic acid Suitable amount (pH 4) Purified water (total amount) 100 mL (about 1.2 mmol / L as iron) Were mixed and dissolved to obtain a liquid preparation.
【0018】 実施例3 クエン酸鉄アンモニウム 100 mg 地黄エキス 500 mg(原生薬換算) キシリトール 10000 mg 精製水 (全量) 100 mL (鉄量として約3.0mmol/L) 上記成分を混合溶解し液剤を得た。Example 3 Ammonium iron citrate 100 mg Ground yellow extract 500 mg (equivalent to crude drug) Xylitol 10,000 mg Purified water (total amount) 100 mL (about 3.0 mmol / L as iron amount) Obtained.
【0019】 実施例4 クエン酸鉄アンモニウム 100 mg 地黄エキス 400 mg(原生薬換算) キシリトール 6000 mg リンゴ酸 適量 (pH4) 精製水 (全量) 100 mL (鉄量として約3.0mmol/L) 上記成分を混合溶解し液剤を得た。Example 4 Ammonium iron citrate 100 mg Ground yellow extract 400 mg (converted to crude drug) Xylitol 6000 mg Malic acid Suitable amount (pH 4) Purified water (total amount) 100 mL (about 3.0 mmol / L as iron) Were mixed and dissolved to obtain a liquid preparation.
【0020】 実施例5 クエン酸鉄アンモニウム 60 mg 地黄エキス 200 mg(原生薬換算) 硝酸チアミン 5 mg リン酸リボフラビンナトリウム 10 mg 塩酸ピリドキシン 10 mg アミノエチルスルホン酸 1500 mg L−アスパラギン酸マグネシウム 1200 mg グルコン酸カルシウム 2500 mg ニコチン酸アミド 20 mg イノシトール 100 mg 無水カフェイン 50 mg ヨクイニン流エキス 2000 mg(原生薬換算) キシリトール 5000 mg 砂糖 5000 mg エリスリトール 1000 mg 安息香酸ナトリウム 70 mg パラオキシ安息香酸ブチル 5 mg パラオキシ安息香酸プロピル 5 mg DL−リンゴ酸 500 mg クエン酸 適量(pH4) ミックスフルーツフレーバー 微量 精製水 (全量) 100 mL (鉄量として1.8mmol/L) 上記成分を混合溶解し液剤を得た。Example 5 Ammonium iron citrate 60 mg Ground yellow extract 200 mg (converted to crude drug) Thiamine nitrate 5 mg Riboflavin sodium phosphate 10 mg Pyridoxine hydrochloride 10 mg Aminoethylsulfonic acid 1500 mg Magnesium L-aspartate 1200 mg Gluconic acid Calcium 2500 mg Nicotinamide 20 mg Inositol 100 mg Anhydrous caffeine 50 mg Yokuinin flow extract 2000 mg (converted to crude drug) Xylitol 5000 mg Sugar 5000 mg Erythritol 1000 mg Sodium benzoate 70 mg Butyl benzoate Propyl benzoate 5 mg Propyl paraoxybenzoate 5 mg DL-malic acid 500 mg Citric acid Appropriate amount (pH 4) Mixed fruit flavor Trace amount Purified water (Total amount) ) 100 mL (1.8 mmol / L as iron amount) The above components were mixed and dissolved to obtain a liquid preparation.
【0021】 比較例1 クエン酸鉄アンモニウム 20 mg 地黄エキス 100 mg(原生薬換算) 精製水 (全量) 100 mL (鉄量として約0.6mmol/L) 上記成分を混合溶解し液剤を得た。Comparative Example 1 Ammonium iron citrate 20 mg Ground yellow extract 100 mg (in terms of crude drug) Purified water (total amount) 100 mL (about 0.6 mmol / L as iron amount) The above components were mixed and dissolved to obtain a liquid preparation.
【0022】 比較例2 クエン酸鉄アンモニウム 40 mg 地黄エキス 200 mg(原生薬換算) リンゴ酸 適量 (pH4) 精製水 (全量) 100 mL (鉄量として約1.8mmol/L) 上記成分を混合溶解し液剤を得た。Comparative Example 2 Ammonium iron citrate 40 mg Ground yellow extract 200 mg (converted to crude drug) Malic acid Suitable amount (pH 4) Purified water (total amount) 100 mL (about 1.8 mmol / L as iron amount) A solution was obtained.
【0023】試験例 上記の実施例1〜4、比較例1及び比較例2の6種類の
鉄成分を配合した液剤について、20人のパネラーによ
り金属味の程度を官能評価した。なお、金属味の評価は
以下の6段階評価で行い、それぞれ平均点を算出した。Test Examples The liquids containing the six iron components of Examples 1 to 4 and Comparative Examples 1 and 2 were organoleptically evaluated for the degree of metallic taste by 20 panelists. In addition, the evaluation of metal taste was performed by the following six-step evaluation, and the average score was calculated for each.
【0024】 評価1:金属味をかなり強く感じる(5点) 評価2:金属味を強く感じる (4点) 評価3:金属味をやや強く感じる (3点) 評価4:金属味を感じる (2点) 評価5:金属味をやや弱く感じる (1点) 評価6:金属味を感じない (0点)。Evaluation 1: Metallic taste is strongly felt (5 points) Evaluation 2: Metallic taste is strongly felt (4 points) Evaluation 3: Metallic taste is somewhat strong (3 points) Evaluation 4: Metallic taste is felt (2 points) Evaluation 5: Metallic taste is slightly weakened (1 point) Evaluation 6: Metallic taste is not felt (0 point).
【0025】結果を表1に示した。表1より明らかなよ
うに、キシリトールの添加により、鉄由来の金属味が顕
著に軽減されることが証明された。The results are shown in Table 1. As is clear from Table 1, it was proved that the addition of xylitol significantly reduced the metallic taste derived from iron.
【0026】[0026]
【表1】 [Table 1]
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 47/10 A61K 47/10 L Fターム(参考) 4C076 AA12 BB01 CC11 CC14 CC21 DD30E DD38T DD41A DD43A EE58T FF52 4C086 AA01 AA02 GA13 HA11 HA20 MA03 MA05 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C088 AB37 AC13 BA08 MA02 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C206 AA01 AA02 CA05 DB03 DB27 JB11 KA13 MA03 MA05 MA37 MA72 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI theme coat ゛ (Reference) A61K 47/10 A61K 47/10 LF term (Reference) 4C076 AA12 BB01 CC11 CC14 CC21 DD30E DD38T DD41A DD43A EE58T FF52 4C086 AA01 AA02 GA13 HA11 HA20 MA03 MA05 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C088 AB37 AC13 BA08 MA02 MA17 MA52 NA09 ZA36 ZA54 ZA55 ZC21 ZC35 4C206 AA01 AA02 CA05 DB03 DB27 JB11 KA13 MA03 Z0537
Claims (4)
ることを特徴とする内服液剤。1. An oral solution containing an iron component, ground yellow and xylitol.
50mmol/Lである請求項1に記載の内服液剤。2. The iron content is 0.05 to 5% in terms of iron content.
The oral liquid preparation according to claim 1, wherein the amount is 50 mmol / L.
トール20mmol以上配合することを特徴とする請求項1
又は2に記載の内服液剤。3. The method according to claim 1, wherein the iron component comprises at least 20 mmol of xylitol per 1 mmol of iron.
Or the oral liquid preparation according to 2.
ニウム、クエン酸鉄ナトリウム及びグルコン酸第一鉄か
ら選ばれる少なくとも1種である請求項1〜3のいずれ
かに記載の内服液剤。4. The oral liquid preparation according to claim 1, wherein the iron component is at least one selected from iron citrate, iron ammonium citrate, sodium iron citrate and ferrous gluconate.
Priority Applications (1)
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JP10351800A JP2000169385A (en) | 1998-12-10 | 1998-12-10 | Internal liquid pharmaceutical preparation |
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JP10351800A JP2000169385A (en) | 1998-12-10 | 1998-12-10 | Internal liquid pharmaceutical preparation |
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JP2000169385A true JP2000169385A (en) | 2000-06-20 |
Family
ID=18419701
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Cited By (5)
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JP2002080347A (en) * | 2000-09-04 | 2002-03-19 | Taisho Pharmaceut Co Ltd | Oral liquid medicine formulated with iron compound |
WO2003024466A1 (en) * | 2001-09-13 | 2003-03-27 | Wakunaga Pharmaceutical Co., Ltd. | Liquid preparation containing crude-drug extract |
JP2005255653A (en) * | 2004-03-15 | 2005-09-22 | Taisho Pharmaceut Co Ltd | Internal liquid medicine formulated with iron compound |
WO2010004916A1 (en) * | 2008-07-08 | 2010-01-14 | 株式会社ゲノム創薬研究所 | Hypoglycemic agent, and food or beverage for prevention of diabetes or amelioration of condition of diabetes comprising same |
JP2020002043A (en) * | 2018-06-27 | 2020-01-09 | 小林製薬株式会社 | Pharmaceutical composition |
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JP2002502817A (en) * | 1998-02-03 | 2002-01-29 | ラボラトワール イノテラ,ソシエテ アノニム | Tablets containing iron as an active ingredient for chewing and licking |
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JPH09194356A (en) * | 1996-01-18 | 1997-07-29 | Taisho Pharmaceut Co Ltd | Internal liquid preparation compounded with iron compound |
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Publication number | Priority date | Publication date | Assignee | Title |
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JP2002080347A (en) * | 2000-09-04 | 2002-03-19 | Taisho Pharmaceut Co Ltd | Oral liquid medicine formulated with iron compound |
WO2003024466A1 (en) * | 2001-09-13 | 2003-03-27 | Wakunaga Pharmaceutical Co., Ltd. | Liquid preparation containing crude-drug extract |
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WO2010004916A1 (en) * | 2008-07-08 | 2010-01-14 | 株式会社ゲノム創薬研究所 | Hypoglycemic agent, and food or beverage for prevention of diabetes or amelioration of condition of diabetes comprising same |
JP5897796B2 (en) * | 2008-07-08 | 2016-03-30 | 株式会社ゲノム創薬研究所 | Hypoglycemic agent and food and drink for preventing diabetes or improving symptoms comprising the same |
JP2020002043A (en) * | 2018-06-27 | 2020-01-09 | 小林製薬株式会社 | Pharmaceutical composition |
JP7360784B2 (en) | 2018-06-27 | 2023-10-13 | 小林製薬株式会社 | pharmaceutical composition |
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